OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Advanced
Search
38
Results
Show all
Save search
Copy query
Show results for
Unknown
(37)
Genomics
(1)
Organisms
Homo sapiens
(1)
Repository
EGA
(1)
Publication Date
Release Date
2021
(6)
2024
(4)
2022
(4)
2019
(4)
2010
(4)
2026
(2)
2025
(2)
2020
(2)
2016
(2)
2011
(2)
2023
(1)
2018
(1)
2014
(1)
2008
(1)
1998
(1)
Previous
page
1 / 4
You're on page
1
page
2
page
3
page
4
Next
page
Sort
by:
Relevance
Page size
10
Structure and distribution of endogenous nonecotropic murine leukemia viruses in wild mice.
Not available
S-EPMC110191
|
biostudies-literature
Cite
Synthesis of modified nucleotide polymers by the poly(U) polymerase Cid1: application to direct RNA sequencing on nanopores.
Not available
S-EPMC8594468
|
biostudies-literature
Cite
A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies.
Not available
S-EPMC6451697
|
biostudies-literature
Cite
Consolidation of the clinical and genetic definition of a
SOX4-
related neurodevelopmental syndrome.
Not available
S-EPMC9433470
|
biostudies-literature
Cite
Genetic diversity of simian immunodeficiency virus encoding HIV-1 reverse transcriptase persists in macaques despite antiretroviral therapy.
Not available
S-EPMC3019993
|
biostudies-literature
Cite
Mouse DNA contamination in human tissue tested for XMRV.
Not available
S-EPMC3019155
|
biostudies-literature
Cite
HIV-1 continues to replicate and evolve in patients with natural control of HIV infection.
Not available
S-EPMC3004307
|
biostudies-literature
Cite
Clones of infected cells arise early in HIV-infected individuals.
Not available
S-EPMC6629130
|
biostudies-literature
Cite
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay.
Not available
S-EPMC6323608
|
biostudies-literature
Cite
Genetic analysis of fin development in zebrafish identifies furin and hemicentin1 as potential novel fraser syndrome disease genes.
Not available
S-EPMC2855323
|
biostudies-literature
Cite
Previous
page
1 / 4
You're on page
1
page
2
page
3
page
4
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets